Canonical Allele Identifier: PA2829437979
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Met14996Val
CA140640
NM_003319.4:c.44986A>G